Philips recalls Transducer C10-3v probes for labeling clarity on useful life in medical ultrasound. No immediate safety risk but requires updated labeling for field use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling its Transducer C10-3v ultrasound probes to clarify their useful life in medical settings. This is a labeling update to help healthcare providers understand how long these probes remain effective during use.
The recall is for labeling clarity to define how long the transducers remain useful in the field. This helps healthcare providers manage the expected lifespan of the probes without posing a safety risk.
Healthcare providers using Philips Transducer C10-3v probes in medical ultrasound procedures are affected. The risk is low as this is a labeling clarification, not a safety hazard.
Check for the Transducer C10-3v model with serial number B2WXV7. This specific probe was recalled for labeling updates to clarify useful life in medical use.
Check the probe's labeling for updated useful life information as per Philips' clarification.
No, this recall is for labeling clarity to define the useful life of the transducers in medical use. There is no safety risk.
Philips is recalling these probes to provide clearer labeling about their expected useful life in the field for healthcare providers.
No, you do not need to stop using the probe. This is a labeling update for better understanding of useful life.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2401-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2401-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.